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 E71.2 Disorder of branched-chain amino-acid metabolism, unspecified
 * E71.3 Disorders of fatty-acid metabolism
 * Excludes1: peroxisomal disorders (E71.5)
 * Refsum's disease (G60.1)
 * Schilder's disease (G37.0)
 * Excludes2: carnitine deficiency due to inborn error of metabolism (E71.42)
 * E71.30 Disorder of fatty-acid metabolism, unspecified
 * E71.31 Disorders of fatty-acid oxidation
 * E71.310 Long chain/very long chain acyl CoA dehydrogenase deficiency
 * LCAD
 * VLCAD
 * E71.311 Medium chain acyl CoA dehydrogenase deficiency
 * MCAD
 * E71.312 Short chain acyl CoA dehydrogenase deficiency
 * SCAD
 * E71.313 Glutaric aciduria type II
 * Glutaric aciduria type II A
 * Glutaric aciduria type II B
 * Glutaric aciduria type II C
 * Excludes1: glutaric aciduria (type 1) NOS (E72.3)
 * E71.314 Muscle carnitine palmitoyltransferase deficiency
 * E71.318 Other disorders of fatty-acid oxidation
 * E71.32 Disorders of ketone metabolism
 * E71.39 Other disorders of fatty-acid metabolism
 * E71.4 Disorders of carnitine metabolism
 * Excludes1: Muscle carnitine palmitoyltransferase deficiency (E71.314)
 * E71.40 Disorder of carnitine metabolism, unspecified
 * E71.41 Primary carnitine deficiency
 * E71.42 Carnitine deficiency due to inborn errors of metabolism
 * Code also associated inborn error or metabolism
 * E71.43 Iatrogenic carnitine deficiency
 * Carnitine deficiency due to:
 * hemodialysis
 * Valproic acid therapy
 * E71.44 Other secondary carnitine deficiency
 * E71.440 Ruvalcaba-Myhre-Smith syndrome
 * E71.448 Other secondary carnitine deficiency
 * E71.5 Peroxisomal disorders
 * Excludes1: Schilder?s disease (G37.0)
 * E71.50 Peroxisomal disorder, unspecified
 * E71.